Variant report

Variant rs12891835
Chromosome Location chr14:105026600-105026601
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105019200-105026600 Enhancers Fetal Brain Male brain
2 chr14:105021000-105029600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr14:105024000-105031400 Enhancers Brain Germinal Matrix brain
4 chr14:105024400-105026600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr14:105024800-105026600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr14:105025200-105027800 Enhancers Fetal Brain Female brain
7 chr14:105025800-105029600 Weak transcription Spleen Spleen
8 chr14:105026600-105026800 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr14:105026600-105026800 Enhancers Lung lung
10 chr14:105026600-105027000 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr14:105026600-105027000 Bivalent Enhancer Fetal Brain Male brain
12 chr14:105026600-105027800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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